MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR
K-Number: K851091 · 1985-04-16
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Device Summary
Frequently Asked Questions
What is the MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR?
MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR is a medical device that received FDA 510(k) clearance on 1985-04-16. The listed applicant is Medtronic Vascular. The 510(k) number is K851091.
When did MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR receive FDA 510(k) clearance?
MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR received FDA 510(k) clearance on 1985-04-16, under 510(k) number K851091.
Who is the listed applicant for MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR?
The FDA 510(k) record lists Medtronic Vascular as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR?
The FDA product code for MEDTRONIC MODEL 5328 PROGRAM-STIMULATOR is JOQ.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Medtronic Vascular as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: JOQ)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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